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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056955inversion1nstd229human GRCh38 chr7: 108,556,029-108,560,814 , GRCh37.p13 chr7: 108,196,473-108,201,258 THAP5
    nsv7049785inversion1nstd229human GRCh38 chr7: 108,552,585-108,561,081 , GRCh37.p13 chr7: 108,193,029-108,201,525 THAP5
    nsv7046492inversion1nstd229human GRCh38 chr7: 108,472,441-108,597,964 , GRCh37.p13 chr7: 108,112,885-108,238,408 PNPLA8, THAP5, 3 more genes
    nsv6837624copy number variation1nstd229human GRCh38 chr7: 108,282,201-108,763,200 , GRCh37.p13 chr7: 107,922,645-108,403,644 DNAJB9, THAP5, 5 more genes
    nsv6835398copy number variation1nstd229human GRCh38 chr7: 108,565,517-108,635,514 , GRCh37.p13 chr7: 108,205,961-108,275,958 LOC105375448, DNAJB9, 1 more genes
    nsv6828603copy number variation1nstd229human GRCh38 chr7: 107,770,269-108,588,414 , GRCh37.p13 chr7: 107,410,714-108,228,858 LOC105375444, DLD, 15 more genes
    nsv6827747copy number variation1nstd229human GRCh38 chr7: 108,568,635-108,572,414 , GRCh37.p13 chr7: 108,209,079-108,212,858 DNAJB9, THAP5
    nsv6818940copy number variation1nstd229human GRCh38 chr7: 108,567,590-108,568,811 , GRCh37.p13 chr7: 108,208,034-108,209,255 DNAJB9, THAP5
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631299copy number variation1nstd224human GRCh37 chr7: 108,202,792-108,213,790 , GRCh38.p12 chr7: 108,562,348-108,573,346 THAP5, DNAJB9
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 more genes
    nsv6313641copy number variation1nstd102humanUncertain significance GRCh37 chr7: 108,099,153-108,503,957 , GRCh38.p12 chr7: 108,458,709-108,863,513 LOC107986836, LOC100419644, 5 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 LHFPL3-AS2, CTB-30L5.1, 233 more genes
    nsv6313503copy number variation1nstd102humanPathogenic GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253 GJC3, LAMB4, 237 more genes
    nsv6136536copy number variation1nstd213human GRCh37 chr7: 107,510,000-112,950,001 , GRCh38.p12 chr7: 107,869,555-113,309,946 NPM1P14, LRRN3, 52 more genes
    nsv6136533copy number variation1nstd213human GRCh37 chr7: 104,130,000-120,060,001 , GRCh38.p12 chr7: 104,489,552-120,419,947 CAPZA2, CFTR, 162 more genes
    nsv6135948copy number variation1nstd213human GRCh37 chr7: 105,420,000-108,740,001 , GRCh38.p12 chr7: 105,779,554-109,099,944 NAMPT, COG5, 49 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
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